Trifluoromethylbenzylphosphonates useful in treating osteoporosis

ABSTRACT

Novel benzylphosphonate compounds of the general formula I: ##STR1## are disclosed as useful in treating bone wasting diseases including postmenopausal osteoporosis in increasing in mammals bone formation and bone mass.

BACKGROUND OF THE INVENTION

Osteoporosis is a bone-wasting disease in which there is an imbalance or uncoupling between the rate of bone formation and resorption resulting in a decrease in total bone mass. As a result of this decrease in bone mass the skeleton becomes weakened and unable to bear the normal weight-bearing stresses. The effects of osteoporosis are generally seen in the weight-bearing part of the skeleton, especially the spine and hips, which can fracture in the absence of trauma. Osteoporosis affects about 24 million people in the United States and 200 million worldwide and is blamed for 2.5 million fractures a year in elderly women. The American Medical Association estimates that 25% of white women will suffer fractures of the hip or spine in their lifetime as a result of osteoporosis.

The current therapies for postmenopausal osteoporosis consist of treatments which are for the most part preventative; estrogen replacement, bisphosphonates, vitamin D metabolites and calcium supplements act to inhibit bone resorption associated with the onset of menopause. Estrogen replacement in these patients is quite effective in reducing further loss of bone mass but it does not induce an increase in bone mass which is needed to reduce fracture risk and pain. These treatments have little utility in the treatment of those patients with existing osteoporosis-induced loss of bone mass who have a high fracture risk and back/joint pain. Post-menopausal women with vertebral bone mass of less than 100 mg/cc would be considered below the "fracture threshold" and would be candidates for treatment with an agent which would increase bone mass and thereby restore lost bone. The present invention focuses on agents which are useful in treating bone wasting diseases by increasing an individuals bone mass and thus reducing or eliminating fracture risk. The therapeutic need for this type of agent is clearly present, especially when one considers the poor patient compliance associated with estrogen replacement therapies.

U.S. Pat. No. 4,610,807 disclosed diethyl 3-trifluoromethylbenzylphosphonate. The compound is not specifically claimed or characterized in the patent but apparently is used in situ as a crude synthetic intermediate towards unrelated compounds with non-medicinal use (fabric whitener). Acids were neither disclosed nor claimed in this reference. Isomeric ortho and para trifluoromethylbenzylphosphonates are similarly disclosed as the esters.

U.S. Pat. No. 2,917,533 discloses several substituted benzylphosphonic acids and esters with utility claims of antihistaminic, antibacterial and herbicidal or plant growth regulatory activity. No 3-CF₃ analog is described.

SUMMARY OF THE INVENTION

Novel benzylphosphonate compounds of the general formula I: ##STR2## wherein R₁, R₂, R₃, R₄, R₅ and R₆ are defined hereinafter have been found to have utility to treat bone wasting diseases including osteoporosis through enhancement of bone calcification, rather than traditional approaches which generally involve inhibition of bone degradation or resorption. The invention is also directed to pharmaceutical compositions containing the compounds of formula I and the methods of treating osteoporosis by administering such compounds and compositions.

DETAILED DESCRIPTION OF THE INVENTION

The present invention is directed to compounds of formula I: ##STR3## wherein R₁ and R₂ are the same or different and are selected from any of hydrogen, C₁ -C₈ alkyl, C₁ -C₈ alkenyl, hydroxyalkyl wherein the alkyl portion is C₁ -C₈, alkoxyalkyl wherein the alkyl portion is C₁ -C₈, aralkyl wherein the alkyl portion is C₁ -C₈, such as benzyl, phenylethyl, phenylpropyl, aryl such as phenyl or aminoalkyl. Aminoalkyl includes substituents of the formula --(CH₂)n--NR₇ R₈, wherein n=2-6 and R₇ and R₈ are the same or different and are selected from any of H, C₁ -C₄ alkyl, aralkyl wherein the alkyl portion in C₁ -C₄ or R₇ and R₈ may be taken together to form a heterocyclic ring having from 5 to 7 ring atoms containing one or more heteroatoms such as N, O and S. Examples of suitable ring systems include piperidino, morpholino, tetrahydroquinolinyl, tetrahydroisoquinolinyl, thiomorpholino and piperazino substituted at the N-4 position by R₉, wherein R₉ is selected from any one of C₁ -C₄ alkyl, or aralkyl wherein the alkyl portion is C₁ -C₄ alkyl or phenyl.

R₃ and R₅ may each be either H or CF₃, with the proviso that only one of R₃ or R₅ may be CF₃ at the same time. R₄ and R₆ may each be H or CF₃, with the proviso that if either or both of R₄ and R₆ are CF₃, neither R₃ nor R₅ may be CF₃ and with the further proviso that R₃ -R₆ may not each be H at the same time.

As used herein the terms "alkyl", "alkenyl" and "alkoxy" when used alone or together with another moiety include both straight and branched alkyl groups.

The term "aryl", as used herein alone or in combination with other terms, indicates aromatic hydrocarbon groups such as a phenyl or naphthyl group. The term "aralkyl" indicates a radical containing a lower C₁ -C₈ alkyl group substituted with an aryl radical.

The compounds of the present invention may also be in the form of pharmaceutically acceptable salts such as sodium, potassium, arginine, lysine, alkyl ammonium such as cyclohexylamine and tris(hydroxyethyl)amine. Basic esters may also be in the form of salts such as hydrochloric, hydrobromic p-toluenesulfonate mesylate, and organic acids such as fumarate.

According to the present invention the compounds may be prepared according to the following general reaction schemes: ##STR4##

As shown, the starting material, a trifluorohalide wherein X is either chloro or bromo and R₃, R₄, R₅ and R₆ are as defined herein is reacted with trialkyl phosphite, under temperatures of about 50° C.-200° C. to give an alkyl trifluorobenzyl phosphonate of formula III. Hydrolysis using an acid such as hydrochloric acid or other suitable acids such as (CH₃)₃ SiBr, HBr, or BBr₃ is used to give the free phosphonic acid of formula IV. Alternatively, the compound of the formula III may be reacted with a base such as potassium or sodium hydroxide, to give the corresponding mono acid product of formula V. Conversion of this mono acid to the acid chloride of formula VI may be accomplished using oxalyl chloride and dimethylformamide or PCl₅. The mixed diester of formula VII may than be prepared from the acid chloride of formula VI by reacting the compound of formula VI with the appropriate alcohol such as diethylaminoethanol, 3-phenylpropanol, hydroxyethylmorpholine, methoxyethanol, ethylene glycol and other well known alcohols.

To prepare the pharmaceutical compositions of this invention, a compound of formula I, as the active ingredient is mixed with a pharmaceutical carrier according to conventional pharmaceutical compounding techniques, which carrier may take a wide variety of forms depending on the form of preparation desired for administration, e.g.; oral, by suppositories, injectable, or parenteral. In preparing the compositions in oral dosage form, any of the usual pharmaceutical media may be employed. Thus, for liquid oral preparations, such as, for example; suspensions, elixirs and solutions, suitable carriers and additives include water, glycols, oils, alcohols, flavorants, perservatives, coloring agents and the like. For solid oral preparations such as, for example; powders, capsules and tablets, suitable carriers and additives include, starches, sugars, diluents, granulating agents, lubricants, binders, disintegrating agents, and the like. Because of their ease of administration, tablets and capsules represent the most advantageous oral dosage unit form in which case, solid pharmaceutical carriers are obviously employed. If desired, tablets may be sugar coated or enteric coated by standard techniques. For suppositories, the carrier will usually comprise cocoa butter. For parenterals, the carrier will usually comprise sterile water, though other ingredients, for example, for purposes such as aiding solubility or for preservation, may be included. Injectable suspensions may also be prepared, in which case appropriate liquid carriers, suspending agents and the like may be employed. The pharmaceutical compositions herein will contain, per unit dosage unit, e.g., tablet, capsule, powder, injection, suppository, teaspoonful and the like, from about 0.1-100 mg/kg. The use of either continuous daily administration or post-periodic dosing may be employed.

The following examples illustrate the present invention but are not deemed to be limiting. Examples 1, 2, 3 and 5-14 illustrate compounds of the present invention. Example 4 illustrates the preparation of an intermediate used to obtain any of the compounds of Examples 5, 6 and 7.

EXAMPLE 1 Diethyl 3-trifluoromethylbenzylphosphonate

A mixture of 3-trifluoromethylbenzyl bromide (5.74 g, 24.0 mmol) and triethyl phosphite (4.98 g, 30 mmol) was heated at reflux under nitrogen for 3 hours. The excess triethyl phosphite was removed by distillation and the crude product obtained was distilled at 140°-145° C. at 4 mm to yield 6.44 g (90.7%) of analytically pure product as a clear liquid, D.C.I.M.S.[MH⁺, 297].

EXAMPLE 2 3-Trifluoromethylbenzylphosphonic acid

Diethyl 3-trifluoromethylbenzylphosphonate (3.0 g, 10.0 mmol) was dissolved in a mixture of 50 mL of conc hydrochloric acid and 1.5 mL of EtOH and was heated at reflux for 17 hours. After cooling the clear reaction mixture in an ice-water mixture, the white crystalline solid which formed was collected to give 2.05 g (84.3%) of the analytical product, mp=163°-164° C.; D.C.I.M.S.[MH⁺,241].

EXAMPLE 3 Ethyl 3-trifluoromethylbenzylphosphonic acid

The diethyl 3-trifluoromethylbenzylphosphonate (10.0 g, 34.0 mmol) was dissolved in a mixture of 300 mL of 75% aqueous ethanol and 18.9 g of KOH and the resultant mixture was heated at reflux for 3 hours. The reaction mixture was poured into H₂ O, acidified with hydrochloric acid, and extracted with CHCl₃ (3×500 mL). The chloroform extract was dried with anhydrous Na₂ SO₄ and evaporated to yield 8.64 g (94.7%) of white solid product, mp=48°-51° C.; D.C.I.M.S.[MH⁺,269].

EXAMPLE 4 3-Trifluromethylbenzylphosphonochloridic acid ethyl ester

Ethyl 3-trifluoromethylbenzylphosphonic acid, (7.46 mmol) was dissolved in 15 mL of CH₂ Cl₂ and cooled to 0° C. under nitrogen. After the oxalyl chloride (0.95 g, 7.46 mmol) had been added, 0.03 mL of DMF was slowly added in 3 portions, and the resultant mixture was stirred at room temperature for 3 hours. Evaporation in vacuo gave the crude chloride which was used without further purification.

EXAMPLE 5 Allyl ethyl 3-trifluoromethylbenzylphosphonate

The 3-trifluoromethylbenzylphosphonochloridic acid ethyl ester of Example 4 (0.2 g, 0.7 mmol) was dissolved in 20 mL of CH₂ Cl₂ and added slowly at 0° C. to a mixture of 1.0 mmol of allyl alcohol and 1.0 of mmol triethylamine in 20 mL of CH₂ Cl₂. The reaction mixture was stirred for 5 hours and then diluted with H₂ O. The aqueous phase was further extracted 3 times with CH₂ Cl₂. The organic extracts were combined and, after drying with anhydrous Na₂ SO₄, were evaporated to give the crude product as an oil. Purification by column chromatography on silica gel using ethyl acetate/hexane (2.5:1) yielded 0.14 g (63%) of analytically pure product as a colorless oil. D.C.I.M.S.[MH⁺ 309].

EXAMPLE 6 Diethylaminoethyl ethyl 3-trifluoromethylbenzylphosphonate

Ethyl 3-trifluoromethylbenzylphosphonic acid, (7.55 g, 28 mmol) was dissolved in 100 mL of CH₂ Cl₂ and cooled to 0° C. under nitrogen. After the oxalyl chloride (28 mmol) had been added, 0.5 mL of DMF was slowly added in 3 portions, and the resultant mixture was stirred at room temperature for 3 hours. Evaporation in vacuo gave the crude acid chloride which was dissolved in 90 mL of CH₂ Cl₂ and added dropwise to a mixture of N,N-diethylaminoethanol (3.29 g, 28 mmol) and triethylamine (3.42 g, 34 mmol) in 60 mL of CH₂ Cl₂ cooled at 0° C. The resultant mixture was allowed to warm to room temperature and stirred for 4 hours. Water was added (100 mL) and the aqueous phase was extracted 3 times with CH₂ Cl₂. The combined organic extracts were dried with anhydrous Na₂ SO₄, and evaporated to give the crude product as an oil. Purification was accomplished through column chromatography on silica gel using CH₂ Cl₂ containing 2% MeOH and 0.1% NH₃ and gave 1.1 g of the analytical product as an orange oil. D.C.I.M.S.[MH⁺, 368].

EXAMPLE 7 Ethyl 3-phenylpropyl 3-trifluoromethylbenzylphosphonate

3-trifluoromethylbenzylphosphonic acid mono ethyl ester (1.5 g, 5.6 mmol) was dissolved in 20 mL of CH₂ Cl₂ and cooled to 0° C. under nitrogen. After the oxalyl chloride (8.46 mmol) had been added, 0.04 mL of DMF was slowly added in 3 portions, and the resultant mixture was stirred at room temperature for 3 hours. Evaporation in vacuo gave the crude acid chloride which was used without further purification. 3-Phenyl-1-propanol (0.76 g, 5.6 mmol), in 15 mL of CH₂ Cl₂, was added to a cold mixture of crude chloro ethyl 3-trifluoromethylbenzylphosphonate (5.6 mmol), triethylamine (0.85 g, 8.4 mmol), and CH₂ Cl₂ (20 mL) cooled at 0° C. The resultant reaction mixture was allowed to stir at room temperature for 4 hours. Evaporation of the volatile components gave a quantitative yield of the expected product. Purification by column chromatography (silica gel, 25% ethyl acetate/hexane) gave 1.66 g (52.3%) of analytically pure product as a pale yellow oil. D.C.I.M.S.[MH⁺, 387].

EXAMPLE 8 Diethyl 4-trifluoromethylbenzylphosphonate

A mixture of 4-trifluoromethylbenzyl bromide (5.68 g, 23.8 mmol) and triethyl phosphite(10.4 g, 63 mmol) was heated at reflux under nitrogen for 5 hours. The excess triethyl phosphite was removed by distillation and the crude product was purified by distillation at 95° C. (0.07 mm Hg.) to give 6.27 g, 89% of the product as an oil. D.C.I.M.S.[MH⁺,297].

EXAMPLE 9 4-Trifluoromethylbenzylphosphonic acid

The diethyl 4-trifluoromethylbenzylphosphonate (3.0 g, 10 mmol) was dissolved in a mixture of 50 mL of conc hydrochloric acid and 5 mL of EtOH and heated at reflux for 17 hours. After cooling the mixture in an ice bath, white crystalline material was collected. Recrystallization of the solid from H₂ O gave 1.80 g, 75% of the analytically pure product: mp=163°-164° C.; D.C.I.M.S.[MH⁺,241].

EXAMPLE 10 Diethyl 2-trifluoromethylbenzylphosphonate

A mixture of 2-trifluoromethylbenzyl chloride (2.0 g, 10.0 mmol) and triethyl phosphite (2.13 g, 13 mmol) was heated at 160° C. under nitrogen for 3 hours. The excess triethyl phosphite was removed by distillation and the crude product obtained was distilled at 87°-90° C. (0.05 mm Hg) and isolated as a colorless oil; yield, 1.68 g, 56.8%; D.C.I.M.S.[MH⁺,297].

EXAMPLE 11 2-Trifluoromethylbenzylphosphonic acid

The diethyl 2-trifluoromethylbenzylphosphonate (1.22 g, 4.12 mmol) was dissolved in a mixture of 50 mL of conc hydrochloric acid and 5 mL of EtOH and was heated at reflux temperature for 17 hours. After cooling the mixture in an ice bath, white crystalline acid was collected to give 0.46 g, 46% of the desired product, mp=190°-192° C.; D.C.I.M.S. [MH⁺, 241].

EXAMPLE 12 Diethyl 3,5-bis(trifluoromethyl)benzylphosphonate

A mixture of 3,5-bis-trifluoromethylbenzyl bromide (5.0 g, 16 mmol) and triethyl phosphite (3.4 g, 20 mmol) was heated at 160° C. for 20 hours. The reaction mixture was cooled and distilled at 83° C. (0.03 mm Hg) to give 2.36 g of the product as a colorless oil in 48% yield. D.C.I.M.S. [MH⁺, 365].

EXAMPLE 13 3,5-Bis(trifluoromethyl)benzylphosphonic acid

Diethyl 3,5-bis(trifluoromethyl)benzylphosphonate (1.0 g, 2.7 mmol) in 15 mL of conc hydrochloric acid and 0.5 mL of ethanol was heated at reflux for 72 hours. The mixture was evaporated to an oily residue which crystallized upon standing to give 0.41 g of the product (49% yield) the as a white solid: mp. 206°-208° C.; D.C.I.M.S. [MH⁺, 309].

EXAMPLE 14 Ethyl morpholinoethyl 3-trifluoromethylbenzylphosphonate

3-Trifluoromethylbenzylphosphonochloric acid ethyl ester (7.0 mmol) in 20 mL of CH₂ Cl₂ is added slowly to a mixture of N-(2-hydroxyethyl)morpholine and triethylamine (7 mmol) in 20 mL of CH₂ Cl₂ cooled in an ice bath. The resultant mixture is allowed to reach room temperature and is stirred for 5 hours. Water is added (100 mL) and the aqueous phase is extracted 3 times with CH₂ Cl₂ (3×100 mL). The combined organic extracts are dried with anhydrous MgSO4, and evaporated to give the desired product.

Compounds of the present invention have utility to treat bone wasting diseases including osteoporosis through enhancement of bone calcification rather than traditional approaches which generally involve inhibition of bone degeneration or resorption. The compounds of the present invention have been evaluated as stimulators of proliferation of osteoblast cell culture which is predictive of enhancement of bone mass and bone formation in vivo.

Osteoblast cell proliferation

The action of select compounds to stimulate osteoblast growth can be measured in culture by estimating the rate of DNA synthesis by the rate of ³ H-thymidine incorporation into DNA. Only cells undergoing mitosis will synthesize new DNA and thus only these cells will incorporate the radiolabelled DNA-specific thymidine. The stimulation of the proliferation and differentiation of bone-forming cells, osteoblasts, is a prerequisite for an increase in bone formation and bone mass. The ability of agents to increase osteoblast proliferation and differentiation can be predicted by their action on cultured osteoblast-line cells in vitro. In this test, mouse (MC3T3-E1) cloned by Sudo et al, Koriyama, Japan) and human (TE-85) osteoblast-line cells (American Type Tissue Culture Collection, #CRL 1543, Rockville, Md.) were cultured in vitro and the effect of various agents was tested on osteoblast cell proliferation. Osteoblasts were isolated and cultured according to literature methods. [J. E. Puzas, R. H. Drivdahl, A. G. Howard, and D. J. Baylink, Proc. Soc. Exper. Biol. Med., 166, 113-122, 1981]. Cells were harvested from large culture flasks where they were allowed to grow to near confluency using trypsin. The cells were plated into 96 well culture plates, 1600 cells in 100 μL per well in Dulbencos Modified Eagle's Medium with 25 mM HEPES buffer, L-glutamine (584 mg/L); D-glucose (4.5 g/L) supplemented with fetal bovine sera (10%); penicillin (100 units/mL) and streptomycin (100 mcg/mL); sodium pyruvate (10 μM final concentration). The cells were allowed to plate overnight in DMEM containing 10% fetal bovine sera at 37° C., in an atmosphere of 5% CO₂ /95% air. Following their placement into 96 ell culture plates all the osteoblast-line cells, either the MC3T3-E1 or the TE-85 cell lines, were allowed an additional 24 hours preincubation period in media containing only 0.1% fetal bovine sera. The next day the test compounds were added and screened at concentrations ranging from 10⁻⁴ to 10⁻⁸ M depending on the study. Twenty hours later, a 20 μL aliquot of media containing 0.4 μCi of ³ H-thymidine was added to each culture well. The cells were then incubated an additional 4 hours. The incubation was terminated by aspirating the media and washing with HBSS (Hank's Balanced Salt Solution). The cells were then treated with 100 μL of 0.5% trypsin and 5.3 mm of EDTA for 30 minutes at room temperature. The cells were then aspirated onto a glass fiber filter and washed with water. The radioactivity on the filters was quantified by liquid scintillation spectroscopy. The rate of ³ H-thymidine incorporation into DNA is then utilized as an index of cell proliferation. The results are shown in Table I expressed as % times control where control is 100%.

                                      TABLE I                                      __________________________________________________________________________      ##STR5##                                                                                                                     Osteoblast Prolif. %                                                           Control                                                                                0.01                    Ex.                                                                               R.sub.1                                                                            R.sub.2  R.sub.3                                                                           R.sub.4                                                                           R.sub.5                                                                           R.sub.6                                                                           FORMULA M.P./B.P.                                                                            [MH+]                                                                               1 μM                                                                            0.1 μM                                                                          μM                                                                             0.001                __________________________________________________________________________                                                               μM                1  Ethyl                                                                              Ethyl    H  CF.sub.3                                                                          H  H  C.sub.12 H.sub.16 F.sub.3 O.sub.3 P                                                    bp 140-145                                                                           297   78 127 124                                                                               159                                                      (4 mm Hg)                                  2  H   H        H  CF.sub.3                                                                          H  H  C.sub.8 H.sub.8 F.sub.3 O.sub.3 P                                                      163-164                                                                              241  299 337 240                                                                               232                  3  H   Ethyl    H  CF.sub.3                                                                          H  H  C.sub.10 H.sub.12 F.sub.3 O.sub.3 P                                                    48- 51                                                                               269   94 117 120                                                                               132                  5  Allyl                                                                              Ethyl    H  CF.sub.3                                                                          H  H  C.sub.13 H.sub.16 F.sub.3 O.sub.3 P                                                    colorless                                                                            309  113 118 127                                                                               127                                                      oil                                        6  Ethyl                                                                              CH.sub.2 CH.sub.2 N(Et).sub.2                                                           H  CF.sub.3                                                                          H  H  C.sub.16 H.sub.20 F.sub.3 NO.sub.3 P                                                   oil   368   84 102  97                                                                               101                  7  Ethyl                                                                              CH.sub.2 CH.sub.2 CH.sub.2 C.sub.6 H.sub.5                                              H  CF.sub.3                                                                          H  H  C.sub.19 H.sub.22 F.sub.3 O.sub.3 P                                                    oil   387   92 113 106                                                                               114                  8  Ethyl                                                                              Ethyl    H  H  CF.sub.3                                                                          H  C.sub.12 H.sub.16 F.sub.3 O.sub.3 P                                                    oil   297  108 100  78                                                                                60                  9  H   H        H  H  CF.sub.3                                                                          H  C.sub.8 H.sub.8 F.sub.3 O.sub.3 P                                                      163-164                                                                              241  195 154 155                                                                               149                  10 Ethyl                                                                              Ethyl    CF.sub.3                                                                          H  H  H  C.sub.12 H.sub.16 F.sub.3 O.sub.3 P                                                    colorless                                                                            297  100  97 161                                                                               193                                                      oil                                        11 H   H        CF.sub.3                                                                          H  H  H  C.sub.8 H.sub.8 F.sub.3 O.sub.3 P                                                      190-192                                                                              241   77 103 102                                                                               116                  12 Ethyl                                                                              Ethyl    H  CF.sub.3                                                                          H  CF.sub.3                                                                          C.sub.13 H.sub.15 F.sub.6 O.sub.3 P                                                    colorless                                                                            365  299 337 240                                                                               231                                                      oil                                        13 H   H        H  CF.sub.3                                                                          H  CF.sub.3                                                                          C.sub.9 H.sub.7 F.sub.6 O.sub.3 P                                                      206-208                                                                              309  --  --  -- --                   __________________________________________________________________________ 

We claim:
 1. A compound represented by the formula I: ##STR6## wherein R₁ and R₂ are the same or different and are selected from any of hydrogen, alkyl, alkenyl, hydroxyalkyl, alkoxyalky, aralkyl, aryl, or aminoalkyl with the proviso that at least one of R₁ and R₂ is aminoalkyl;wherein aminoalkyl is --(CH₂)n--N R₇ R₈ wherein n=2-6 and R₇ and R₈ are the same or different and are selected from any of H, alkyl, aralkyl; wherein R₃ and R₅ may each be either H of CF₃, with the proviso that only one of R₃ or R₅ may be CF₃ at the same time; wherein R₄ and R₆ may each be H or CF₃, with the proviso that if either or both of R₄ and R₆ are CF₃, neither R₃ nor R₅ may be CF₃, with the further proviso that R₃ -R₆ may not each be H at the same time; or pharmaceutically acceptable salts thereof.
 2. The compound of claim 1, wherein the compound is diethylaminoethyl ethyl 3-trifluoromethylbenzylphosphonate. 